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1. Xiangfei Han, et al. Paclitaxel-paclitaxel Prodrug Nanoassembly as a Versatile Nanoplatform for Combinational Cancer Therapy, ACS Applied Materials & Interfaces, 2016, 8(49),33506-33513£¨IF=7.145£©2. Guolian Ren, et al. A unique highly hydrophobic anticancer prodrug self-assembled nanomedicine for cancer therapy,Nanomedicine: Nanotechnology, Biology and Medicine, 2016,12:2273-2282(IF=5.671)3. Peng Xue, et al. Redox-sensitive citronellol-cabazitaxel conjugate: maintained in vitro cytotoxicity and self-assembled as multifunctional nanomedicine, Bioconjugate Chemistry, 2016,27(5):1360-72(IF=4.5)4. Guolian Ren, et al.Docetaxel prodrug liposomes for tumor therapy: characterization, in vitro and in vivo evaluation, Drug Delivery,2016, 23(4):1272-81(IF=4.843)5. Jing Wang, et al. Comparison of two kinds of docetaxel-vitamin E prodrugs: in vitro evaluation and in vivo antitumor activity,International Journal of Pharmaceutics, 2016, 505(1-2):352-60(IF=3.994)6. Qiang Fu, et al. Programmed Hydrolysis in Designing Paclitaxel Prodrug for NanocarrierAssemby, Scientific Reports, 2015, 5,12023:1-10 (IF=5.228)7. Yongjun Wang, et al. Molecular-matched materials for anticancer drug delivery and imaging, Nanomedicine(Lond.), 2015,10(19):3003¨C3013(IF=5.413)8. Yongjun Wang, et al. Disulfide Bond Bridge Inse rtion Turns Hydrophobic Anticancer Prodrugs into Self-Assembled Nanomedicines. Nano Letters. 201414:5577-5583.£¨IF=13.592£©9. Yongjun Wang, et al. Shape-Controlled Paclitaxel Nanoparticles with Multiple Morphologies: Rod-Shaped, Worm-Like, Spherical, and Fingerprint-Like. Molecular pharmaceutics. 2014.£¨IF=4.78£©10. Jingling Tang, et al. Key structure of brij for overcoming multidrug resistance in cancer. Biomacromolecules. 201314:424-430.£¨IF=5.78£©Ö÷±à»ò²Î±àµÄ½Ì²Ä¡¢×¨Öø1.¹¤ÒµÒ©¼Áѧ£¬²Î±à£¬ÖйúÒ½Ò©¿Æ¼¼³ö°æÉ磬2014Äê2.ҩѧöλÔÓéÀֵǼÈë¿ÚÏÂÔØÂÛÎÄ׫дҪÇóÓë·¶Àý£¬²Î±à£¬ÖйúÒ½Ò©¿Æ¼¼³ö°æÉ磬2012Äê3.ÄÉÃ×Á£¸øÒ©ÏµÍ³£¬Ö÷Ò룬¿ÆÑ§³ö°æÉ磬2011Äê4.Ò©¼Áѧ£¬²Î±à£¬ÉϺ£¿ÆÑ§¼¼Êõ³ö°æÉ磬2011Äê5.»·ºý¾«°üºÏÎï¼¼Êõ£¬²Î±à£¬ÈËÃñÎÀÉú³ö°æÉ磬2008Äê
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